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Impact of deep or ovarian endometriosis on pelvic pain and quality of life: prospective cross-sectional ultrasound study. 深部或卵巢子宫内膜异位症对盆腔疼痛和生活质量的影响:前瞻性横断面超声波研究。
IF 6.1 1区 医学 Q1 ACOUSTICS Pub Date : 2025-03-01 Epub Date: 2025-01-14 DOI: 10.1002/uog.29150
P Chaggar, T Tellum, N Thanatsis, L V De Braud, T Setty, D Jurkovic

Objective: To assess whether premenopausal women diagnosed with deep or ovarian endometriosis on transvaginal sonography (TVS) were more likely to suffer from dyspareunia and pelvic pain symptoms, and have a lower quality of life, compared to women without sonographically diagnosed deep or ovarian endometriosis.

Methods: This was a prospective, cross-sectional study carried out between February 2019 and October 2020 at the general gynecology clinic at University College London Hospital, London, UK. All premenopausal women aged 18-50 years, who were examined consecutively by a single experienced examiner and underwent a detailed TVS scan, were eligible for inclusion. Pregnant women and those who had received a previous diagnosis of endometriosis or who had experienced a hysterectomy or unilateral/bilateral oophorectomy were excluded. Sonographic findings consistent with deep or ovarian endometriosis were noted. All women completed the British Society of Gynaecological Endoscopy pelvic pain questionnaire. The primary outcome was to determine whether women with sonographic evidence of endometriosis were more likely to experience moderate-to-severe levels of dyspareunia (score of ≥ 4 on an 11-point numerical rating scale (NRS)). Secondary outcomes included assessing moderate-to-severe levels of other pelvic pain symptoms (NRS score of ≥ 4), bowel symptoms (score of ≥ 2 on a 5-point Likert scale) and quality of life, which was measured using the EuroQol-5D-3L (EQ-5D) questionnaire. The number of women with pain scores ≥ 4 and bowel scores ≥ 2, as well as the mean EQ-5D scores, were compared between the group with and that without sonographic evidence of endometriosis using logistic regression analysis, and multivariable analysis was used to adjust for demographic and clinical variables.

Results: A total of 514 women were included in the final study population, of whom 146 (28.4%) were diagnosed with deep or ovarian endometriosis on TVS. On multivariable analysis, the presence of moderate-to-severe dyspareunia was not found to be associated with endometriosis. Moderate-to-severe dyspareunia was significantly associated with lower age (odds ratio (OR), 0.70 (95% CI, 0.56-0.89); P = 0.003) and a history of migraine (OR, 3.52 (95% CI, 1.42-8.77); P = 0.007), and it occurred significantly less frequently in women with non-endometriotic ovarian cysts (OR, 0.47 (95% CI, 0.28-0.78); P = 0.003). There was also a trend towards a positive association between anxiety/depression and moderate-to-severe dyspareunia (OR, 1.94 (95% CI, 0.93-4.03); P = 0.08). Following multivariable analysis, the only symptoms that were significantly more common in women with endometriosis compared to those without were menstrual dyschezia (OR, 2.44 (95% CI, 1.59-3.78); P < 0.001) and difficulty emptying the bladder (OR, 2.56 (95% CI, 1.52-4.31); P < 0.001). Although not reaching statistical significance on multivariable

目的:评价经阴道超声(TVS)诊断为深部或卵巢子宫内膜异位症的绝经前妇女与未诊断为深部或卵巢子宫内膜异位症的妇女相比,是否更容易出现性交困难和盆腔疼痛症状,并有较低的生活质量。方法:这是一项前瞻性横断面研究,于2019年2月至2020年10月在英国伦敦伦敦大学学院医院的普通妇科诊所进行。所有年龄在18-50岁的绝经前妇女,由一位经验丰富的检查人员连续检查并进行详细的TVS扫描,均符合纳入条件。孕妇和以前被诊断为子宫内膜异位症或经历过子宫切除术或单侧/双侧卵巢切除术的人被排除在外。超声检查结果与深部或卵巢子宫内膜异位症一致。所有女性都完成了英国妇科内镜学会骨盆疼痛问卷调查。主要结局是确定有子宫内膜异位症超声证据的妇女是否更有可能经历中度至重度的性交困难(在11分数值评定量表(NRS)中得分≥4分)。次要结局包括评估中度至重度其他盆腔疼痛症状(NRS评分≥4)、肠道症状(5分Likert评分≥2)和生活质量,生活质量采用EuroQol-5D-3L (EQ-5D)问卷进行测量。采用logistic回归分析比较有和无子宫内膜异位症超声证据组疼痛评分≥4分、肠道评分≥2分的妇女人数以及EQ-5D平均评分,并采用多变量分析调整人口统计学和临床变量。结果:最终纳入研究人群的女性共有514名,其中146名(28.4%)被TVS诊断为深部或卵巢子宫内膜异位症。在多变量分析中,未发现中度至重度性交困难与子宫内膜异位症相关。中度至重度性交困难与较低年龄显著相关(优势比(OR), 0.70 (95% CI, 0.56-0.89);P = 0.003)和偏头痛史(OR, 3.52 (95% CI, 1.42-8.77);P = 0.007),非子宫内膜异位性卵巢囊肿患者的发生率明显较低(OR, 0.47 (95% CI, 0.28-0.78);p = 0.003)。焦虑/抑郁与中重度性交困难之间也有正相关的趋势(OR, 1.94 (95% CI, 0.93-4.03);p = 0.08)。多变量分析后,子宫内膜异位症患者与无子宫内膜异位症患者相比,唯一明显更常见的症状是月经紊乱(OR, 2.44 (95% CI, 1.59-3.78);结论:大多数盆腔疼痛症状在有子宫内膜异位症和没有子宫内膜异位症超声证据的妇女之间没有显著差异,表明子宫内膜异位症可能并不总是盆腔疼痛的来源,即使存在。这突出了在考虑手术前排除症状性子宫内膜异位症患者疼痛的其他原因,并提供适当的患者咨询的必要性。©2024作者。妇产科学超声由John Wiley & Sons Ltd代表国际妇产科学超声学会出版。
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引用次数: 0
Intra- and interobserver agreement of proposed objective transvaginal ultrasound image-quality scoring system for use in artificial intelligence algorithm development. 用于人工智能算法开发的客观经阴道超声图像质量评分系统的内部和内部观察者协议。
IF 6.1 1区 医学 Q1 ACOUSTICS Pub Date : 2025-03-01 Epub Date: 2025-01-24 DOI: 10.1002/uog.29178
A Deslandes, J C Avery, H-T Chen, M Leonardi, S Knox, G Lo, R O'Hara, G Condous, M L Hull

Objectives: The development of valuable artificial intelligence (AI) tools to assist with ultrasound diagnosis depends on algorithms developed using high-quality data. This study aimed to test the intra- and interobserver agreement of a proposed image-quality scoring system to quantify the quality of gynecological transvaginal ultrasound (TVS) images, which could be used in clinical practice and AI tool development.

Methods: A proposed scoring system to quantify TVS image quality was created following a review of the literature. This system involved a score of 1-4 (2 = poor, 3 = suboptimal and 4 = optimal image quality) assigned by a rater for individual ultrasound images. If the image was deemed inaccurate, it was assigned a score of 1, corresponding to 'reject'. Six professionals, including two radiologists, two sonographers and two sonologists, reviewed 150 images (50 images of the uterus and 100 images of the ovaries) obtained from 50 women, assigning each image a score of 1-4. The review of all images was repeated a second time by each rater after a period of at least 1 week. Mean scores were calculated for each rater. Overall interobserver agreement was assessed using intraclass correlation coefficient (ICC), and interobserver agreement between paired professionals and intraobserver agreement for all professionals were assessed using weighted Cohen's kappa and ICC.

Results: Poor levels of interobserver agreement were obtained between the six raters for all 150 images (ICC, 0.480 (95% CI, 0.363-0.586)), as well as for assessment of the uterine images only (ICC, 0.359 (95% CI, 0.204-0.523)). Moderate agreement was achieved for the ovarian images (ICC, 0.531 (95% CI, 0.417-0.636)). Agreement between the paired sonographers and sonologists was poor for all images (ICC, 0.336 (95% CI, -0.078 to 0.619) and 0.425 (95% CI, 0.014-0.665), respectively), as well as when images were grouped into uterine images (ICC, 0.253 (95% CI, -0.097 to 0.577) and 0.299 (95% CI, -0.094 to 0.606), respectively) and ovarian images (ICC, 0.400 (95% CI, -0.043 to 0.669) and 0.469 (95% CI, 0.088-0.689), respectively). Agreement between the paired radiologists was moderate for all images (ICC, 0.600 (95% CI, 0.487-0.693)) and for their assessment of uterine images (ICC, 0.538 (95% CI, 0.311-0.707)) and ovarian images (ICC, 0.621 (95% CI, 0.483-0.728)). Weak-to-moderate intraobserver agreement was seen for each of the raters with weighted Cohen's kappa ranging from 0.533 to 0.718 for all images and from 0.467 to 0.751 for ovarian images. Similarly, for all raters, the ICC indicated moderate-to-good intraobserver agreement for all images overall (ICC ranged from 0.636 to 0.825) and for ovarian images (ICC ranged from 0.596 to 0.862). Slightly better intraobserver agreement was seen for uterine images, with weighted Cohen's kappa ranging from 0.568 to 0.808 indicating weak-to-strong agreement, and ICC ranging

目标:开发有价值的人工智能(AI)工具来辅助超声诊断取决于使用高质量数据开发的算法。本研究旨在测试拟用于量化妇科经阴道超声(TVS)图像质量的图像质量评分系统的观察者内部和观察者之间的一致性,该系统可用于临床实践和人工智能工具开发:方法:在查阅文献后,我们提出了一套用于量化 TVS 图像质量的评分系统。该系统由评分员对单个超声图像进行 1-4 级评分(2 = 差,3 = 次优,4 = 最佳图像质量)。如果认为图像不准确,则打 1 分,即 "拒绝"。包括两名放射科医生、两名超声技师和两名超声学家在内的六名专业人员审查了从 50 名妇女处获得的 150 张图像(50 张子宫图像和 100 张卵巢图像),并给每张图像打 1-4 分。至少一周后,每位评分者再次复查所有图像。计算每位评分者的平均分。使用类内相关系数(ICC)评估观察者之间的总体一致性,使用加权科恩卡帕(Cohen's kappa)和 ICC 评估配对专业人员之间的观察者一致性和所有专业人员的观察者内部一致性:结果:六位评分员在所有 150 张图像(ICC,0.480(95% CI,0.363-0.586))以及仅在子宫图像(ICC,0.359(95% CI,0.204-0.523))的评估中的观察者间一致性较差。卵巢图像的一致性为中等(ICC,0.531(95% CI,0.417-0.636))。配对超声技师和超声科医生在所有图像上的一致性较差(ICC,分别为 0.336 (95% CI, -0.078 to 0.619) 和 0.425 (95% CI, 0.014-0.665)),当图像分组为子宫图像时也是如此(ICC,0.253(95% CI,-0.097 至 0.577)和 0.299(95% CI,-0.094 至 0.606))以及卵巢图像(ICC,分别为 0.400(95% CI,-0.043 至 0.669)和 0.469(95% CI,0.088 至 0.689))。对于所有图像(ICC,0.600(95% CI,0.487-0.693))以及子宫图像(ICC,0.538(95% CI,0.311-0.707))和卵巢图像(ICC,0.621(95% CI,0.483-0.728))的评估,配对放射科医生之间的一致性为中等。所有图像的加权科恩卡帕(Cohen's kappa)范围为 0.533 至 0.718,卵巢图像的加权科恩卡帕(Cohen's kappa)范围为 0.467 至 0.751。同样,所有评分者的 ICC 显示,所有图像(ICC 在 0.636 到 0.825 之间)和卵巢图像(ICC 在 0.596 到 0.862 之间)的观察者内部一致性为中等到良好。子宫图像的观察者内部一致性稍好,加权科恩卡帕(Cohen's kappa)在 0.568 到 0.808 之间,表明一致性从弱到强,ICC 在 0.546 到 0.893 之间,表明一致性从中度到良好。所有测量结果均具有统计学意义(P 结论):建议的图像质量评分系统的观察者间一致性为差到中等,观察者内一致性大多为弱到中等。尽管鉴于超声解读的高度主观性,能否实现图像质量的量化仍是未知数,但可能需要对评分系统进行更多改进,以提高一致性。虽然有些人工智能系统可以容忍标记噪声,但大多数系统更倾向于干净(高质量)的数据。因此,需要创新的数据标记策略。©2025年作者。妇产科超声》由 John Wiley & Sons Ltd 代表国际妇产科超声学会出版。
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引用次数: 0
Reply. 回复。
IF 6.1 1区 医学 Q1 ACOUSTICS Pub Date : 2025-03-01 Epub Date: 2025-01-24 DOI: 10.1002/uog.29157
M L Larsen, S Kumar
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引用次数: 0
Angiogenic factors alone or in combination with ultrasound Doppler criteria for risk classification among late-onset small fetuses with or without pre-eclampsia. 血管生成因子单独或联合超声多普勒标准对伴或不伴先兆子痫的晚发型小胎儿的危险分级
IF 6.1 1区 医学 Q1 ACOUSTICS Pub Date : 2025-03-01 Epub Date: 2025-01-30 DOI: 10.1002/uog.29181
L Youssef, F Crispi, S Paolucci, J Miranda, S Lobmaier, F Crovetto, F Figueras, E Gratacos
<p><strong>Objective: </strong>To investigate the prognostic value of maternal angiogenic factors in late-onset small fetuses, alone or in combination with the ultrasound and Doppler parameters currently used for the classification of low-risk small-for-gestational-age (SGA) fetuses or high-risk fetal growth restriction (FGR), overall and according to the presence or absence of pre-eclampsia.</p><p><strong>Methods: </strong>This was a prospective cohort study of women with a singleton pregnancy with a diagnosis of late-onset fetal smallness (defined as birth weight < 10<sup>th</sup> centile) and a gestational age of ≥ 34 weeks at delivery. Ultrasound assessment of estimated fetal weight (EFW) and Doppler assessment of uterine artery pulsatility index (UtA-PI) and cerebroplacental ratio (CPR) were performed every 1-2 weeks. Biochemical analysis of the angiogenic factors placental growth factor (PlGF) and soluble fms-like tyrosine kinase-1 (sFlt-1) in maternal peripheral venous blood samples was performed using enzyme-linked immunosorbent assay within 1-2 weeks after diagnosis of SGA or FGR. The primary outcome was adverse perinatal outcome, defined as a composite of emergency Cesarean section for non-reassuring fetal status, metabolic acidosis (umbilical artery pH < 7.0), neonatal unit admission and/or perinatal death. The predictive value of EFW < 3<sup>rd</sup> centile, Doppler parameters (UtA-PI > 95<sup>th</sup> centile and CPR < 5<sup>th</sup> centile) and sFlt-1/PlGF ratio > 95<sup>th</sup> centile, alone or in combination, was assessed using logistic regression analysis in the overall population and stratified by presence or absence of pre-eclampsia developing at any time before delivery.</p><p><strong>Results: </strong>Among the 602 included cases, 91 (15.1%) developed pre-eclampsia and 511 (84.9%) did not. In the overall study population, all parameters were associated independently with adverse perinatal outcome: EFW < 3<sup>rd</sup> centile (adjusted odds ratio (aOR), 2.58 (95% CI, 1.67-4.00)), UtA-PI > 95<sup>th</sup> centile (aOR, 1.92 (95% CI, 1.25-2.94)), CPR < 5<sup>th</sup> centile (aOR, 2.35 (95% CI, 1.46-3.78)) and sFlt-1/PlGF ratio > 95<sup>th</sup> centile (aOR, 1.71 (95% CI, 1.09-2.69)). Only sFlt-1/PlGF ratio > 95<sup>th</sup> centile was associated independently with adverse perinatal outcome in cases with pre-eclampsia, whereas in those without pre-eclampsia, only EFW < 3<sup>rd</sup> centile and CPR < 5<sup>th</sup> centile were associated independently with adverse perinatal outcome. In the overall population, the detection rate (DR) and false-positive rate for adverse perinatal outcome were, respectively: 39.8% (95% CI, 31.7-47.9%) and 16.9% (95% CI, 10.7-23.1%) for sFlt-1/PlGF ratio > 95<sup>th</sup> centile alone; 86.8% (95% CI, 83.4-90.2%) and 61.9% (95% CI, 57.1-66.7%) for a combined model of EFW < 3<sup>rd</sup> centile, UtA-PI > 95<sup>th</sup> centile and CPR < 5<sup>th</sup> centile; 81.3% (95% CI, 77.3-85.3%) a
目的:探讨母体血管生成因子在迟发性小胎中的预后价值,单独或联合目前用于低危小胎龄(SGA)胎或高危胎生受限(FGR)胎的超声和多普勒参数,总体上并根据是否存在先兆子痫。方法:这是一项前瞻性队列研究,研究对象为诊断为晚发型胎儿小(定义为出生体重百分位)且分娩时胎龄≥34周的单胎妊娠妇女。超声评估胎儿体重(EFW),多普勒评估子宫动脉搏动指数(UtA-PI)和脑胎盘比(CPR)每1-2周。在诊断为SGA或FGR后1-2周内,采用酶联免疫吸附法对母体外周静脉血中血管生成因子胎盘生长因子(PlGF)和可溶性纤维样酪氨酸激酶-1 (sFlt-1)进行生化分析。主要结局是不良的围产期结局,定义为因胎儿状态不稳定而紧急剖宫产、代谢性酸中毒(脐动脉pH为1百分位,多普勒参数(UtA-PI为1百分位,95百分位,CPR为1百分位)和sFlt-1/PlGF比值(95百分位,单独或联合)的组合,在总体人群中使用logistic回归分析进行评估,并根据分娩前任何时间是否发生先兆子痫进行分层。结果:602例患者中,91例(15.1%)出现先兆子痫,511例(84.9%)未出现先兆子痫。在整个研究人群中,所有参数都与不良围产期结局独立相关:EFW rd百分位(校正优势比(aOR), 2.58 (95% CI, 1.67-4.00)), UtA-PI > 95百分位(aOR, 1.92 (95% CI, 1.25-2.94)), CPR第1百分位(aOR, 2.35 (95% CI, 1.46-3.78))和sFlt-1/PlGF比值> 95百分位(aOR, 1.71 (95% CI, 1.09-2.69))。在子痫前期患者中,只有sFlt-1/PlGF比值bbbb95百分位与不良围产期结局独立相关,而在无子痫前期患者中,只有EFW百分位和CPR百分位与不良围产期结局独立相关。在总体人群中,不良围产期结局的检出率(DR)和假阳性率分别为:仅第95百分位的sFlt-1/PlGF比值为39.8% (95% CI, 31.7-47.9%)和16.9% (95% CI, 10.7-23.1%);EFW rd百分位、UtA-PI bbb95百分位和CPR第th百分位的组合模型为86.8% (95% CI, 83.4-90.2%)和61.9% (95% CI, 57.1-66.7%);EFW rd百分位和sFlt-1/PlGF比值bbb95百分位的组合模型分别为81.3% (95% CI, 77.3-85.3%)和52.3% (95% CI, 47.1-57.5%);包括上述所有观测参数的组合模型为88.5% (95% CI, 85.4-91.6%)和64.5% (95% CI, 59.8-69.2%)。结论:单用sFlt-1/PlGF比值对围产期不良结局的预测价值较低,但联合EFW时,其预测效果与EFW联合多普勒参数相似。将sFlt-1/PlGF比值与EFW和多普勒标准相结合,对不良围产期结局的DR最高,此外,可能有助于识别胎儿小的妊娠中即将发生的先兆子痫。这些发现支持将血管生成因子作为目前用于识别晚发型小胎儿高危FGR的附加标准,但不支持将其作为独立的生物标志物。©2025国际妇产科超声学会。
{"title":"Angiogenic factors alone or in combination with ultrasound Doppler criteria for risk classification among late-onset small fetuses with or without pre-eclampsia.","authors":"L Youssef, F Crispi, S Paolucci, J Miranda, S Lobmaier, F Crovetto, F Figueras, E Gratacos","doi":"10.1002/uog.29181","DOIUrl":"10.1002/uog.29181","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To investigate the prognostic value of maternal angiogenic factors in late-onset small fetuses, alone or in combination with the ultrasound and Doppler parameters currently used for the classification of low-risk small-for-gestational-age (SGA) fetuses or high-risk fetal growth restriction (FGR), overall and according to the presence or absence of pre-eclampsia.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;This was a prospective cohort study of women with a singleton pregnancy with a diagnosis of late-onset fetal smallness (defined as birth weight &lt; 10&lt;sup&gt;th&lt;/sup&gt; centile) and a gestational age of ≥ 34 weeks at delivery. Ultrasound assessment of estimated fetal weight (EFW) and Doppler assessment of uterine artery pulsatility index (UtA-PI) and cerebroplacental ratio (CPR) were performed every 1-2 weeks. Biochemical analysis of the angiogenic factors placental growth factor (PlGF) and soluble fms-like tyrosine kinase-1 (sFlt-1) in maternal peripheral venous blood samples was performed using enzyme-linked immunosorbent assay within 1-2 weeks after diagnosis of SGA or FGR. The primary outcome was adverse perinatal outcome, defined as a composite of emergency Cesarean section for non-reassuring fetal status, metabolic acidosis (umbilical artery pH &lt; 7.0), neonatal unit admission and/or perinatal death. The predictive value of EFW &lt; 3&lt;sup&gt;rd&lt;/sup&gt; centile, Doppler parameters (UtA-PI &gt; 95&lt;sup&gt;th&lt;/sup&gt; centile and CPR &lt; 5&lt;sup&gt;th&lt;/sup&gt; centile) and sFlt-1/PlGF ratio &gt; 95&lt;sup&gt;th&lt;/sup&gt; centile, alone or in combination, was assessed using logistic regression analysis in the overall population and stratified by presence or absence of pre-eclampsia developing at any time before delivery.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Among the 602 included cases, 91 (15.1%) developed pre-eclampsia and 511 (84.9%) did not. In the overall study population, all parameters were associated independently with adverse perinatal outcome: EFW &lt; 3&lt;sup&gt;rd&lt;/sup&gt; centile (adjusted odds ratio (aOR), 2.58 (95% CI, 1.67-4.00)), UtA-PI &gt; 95&lt;sup&gt;th&lt;/sup&gt; centile (aOR, 1.92 (95% CI, 1.25-2.94)), CPR &lt; 5&lt;sup&gt;th&lt;/sup&gt; centile (aOR, 2.35 (95% CI, 1.46-3.78)) and sFlt-1/PlGF ratio &gt; 95&lt;sup&gt;th&lt;/sup&gt; centile (aOR, 1.71 (95% CI, 1.09-2.69)). Only sFlt-1/PlGF ratio &gt; 95&lt;sup&gt;th&lt;/sup&gt; centile was associated independently with adverse perinatal outcome in cases with pre-eclampsia, whereas in those without pre-eclampsia, only EFW &lt; 3&lt;sup&gt;rd&lt;/sup&gt; centile and CPR &lt; 5&lt;sup&gt;th&lt;/sup&gt; centile were associated independently with adverse perinatal outcome. In the overall population, the detection rate (DR) and false-positive rate for adverse perinatal outcome were, respectively: 39.8% (95% CI, 31.7-47.9%) and 16.9% (95% CI, 10.7-23.1%) for sFlt-1/PlGF ratio &gt; 95&lt;sup&gt;th&lt;/sup&gt; centile alone; 86.8% (95% CI, 83.4-90.2%) and 61.9% (95% CI, 57.1-66.7%) for a combined model of EFW &lt; 3&lt;sup&gt;rd&lt;/sup&gt; centile, UtA-PI &gt; 95&lt;sup&gt;th&lt;/sup&gt; centile and CPR &lt; 5&lt;sup&gt;th&lt;/sup&gt; centile; 81.3% (95% CI, 77.3-85.3%) a","PeriodicalId":23454,"journal":{"name":"Ultrasound in Obstetrics & Gynecology","volume":" ","pages":"317-324"},"PeriodicalIF":6.1,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143068194","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comprehensive prenatal ultrasound for surgical risk assessment: differentiating placenta accreta spectrum from uterine scar dehiscence for improved clinical decision-making. 用于手术风险评估的产前综合超声波检查:区分胎盘早剥和子宫瘢痕开裂以改进临床决策。
IF 6.1 1区 医学 Q1 ACOUSTICS Pub Date : 2025-02-01 Epub Date: 2024-11-07 DOI: 10.1002/uog.29138
R A Aryananda, T K Adu-Bredu
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引用次数: 0
Posterior complex: clue for suspicion of partial agenesis of corpus callosum at fetal brain screening. 后复合体:胎儿脑筛查中怀疑胼胝体部分缺失的线索。
IF 6.1 1区 医学 Q1 ACOUSTICS Pub Date : 2025-02-01 Epub Date: 2024-10-30 DOI: 10.1002/uog.29136
F Viñals, F Correa
{"title":"Posterior complex: clue for suspicion of partial agenesis of corpus callosum at fetal brain screening.","authors":"F Viñals, F Correa","doi":"10.1002/uog.29136","DOIUrl":"10.1002/uog.29136","url":null,"abstract":"","PeriodicalId":23454,"journal":{"name":"Ultrasound in Obstetrics & Gynecology","volume":" ","pages":"239-241"},"PeriodicalIF":6.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142547754","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
ISUOG Practice Guidelines (updated): role of ultrasound in twin pregnancy. ISUOG实践指南(更新):超声在双胎妊娠中的作用。
IF 6.1 1区 医学 Q1 ACOUSTICS Pub Date : 2025-02-01 Epub Date: 2025-01-15 DOI: 10.1002/uog.29166
A Khalil, A Sotiriadis, A Baschat, A Bhide, E Gratacós, K Hecher, L Lewi, L J Salomon, B Thilaganathan, Y Ville
{"title":"ISUOG Practice Guidelines (updated): role of ultrasound in twin pregnancy.","authors":"A Khalil, A Sotiriadis, A Baschat, A Bhide, E Gratacós, K Hecher, L Lewi, L J Salomon, B Thilaganathan, Y Ville","doi":"10.1002/uog.29166","DOIUrl":"10.1002/uog.29166","url":null,"abstract":"","PeriodicalId":23454,"journal":{"name":"Ultrasound in Obstetrics & Gynecology","volume":" ","pages":"253-276"},"PeriodicalIF":6.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11788470/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143012364","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Performance evaluation of computerized antepartum fetal heart rate monitoring: Dawes-Redman algorithm at term. 计算机产前胎儿心率监测的性能评价:足月Dawes-Redman算法。
IF 6.1 1区 医学 Q1 ACOUSTICS Pub Date : 2025-02-01 DOI: 10.1002/uog.29167
G Davis Jones, B Albert, W Cooke, M Vatish
<p><strong>Objectives: </strong>To assess the effectiveness of the Dawes-Redman algorithm in identifying fetal wellbeing at term by analyzing 30 years of retrospective clinical data, comparing normal and adverse pregnancy outcomes, evaluating key metrics and testing its performance when used 0-48 h before delivery.</p><p><strong>Methods: </strong>Antepartum fetal heart rate (FHR) traces from term singleton pregnancies at 37 + 0 to 41 + 6 weeks' gestation obtained between 1991 and 2024 were extracted from the Oxford University Hospitals database. Traces with > 30% of their signal information missing or with incomplete Dawes-Redman analyses were excluded. Only traces performed within 48 h prior to delivery were considered. A cohort of pregnancies with subsequent normal pregnancy outcome (NPO) was established using rigorous inclusion and exclusion criteria. Another cohort of pregnancies with adverse pregnancy outcome (APO) was developed if the neonate experienced at least one of seven APOs after delivery. Propensity score matching (PSM) facilitated a balanced comparison between NPO and APO cohorts using six factors: gestational age at FHR monitoring, fetal sex, maternal body mass index at presentation, maternal age at delivery, parity and time interval between FHR trace and delivery. FHR traces were categorized as either 'criteria met' (indicating fetal wellbeing) or 'criteria not met' (indicating a need for further evaluation) according to the Dawes-Redman algorithm, which informed the evaluation of predictive performance metrics. Performance was assessed using accuracy, sensitivity, specificity, positive predictive value, and negative predictive value (NPV) adjusted for various population risk prevalences of APO.</p><p><strong>Results: </strong>A balanced dataset of 3316 antepartum FHR traces was developed with PSM (standardized mean difference < 0.10). The Dawes-Redman algorithm showed a high specificity of 90.7% (95% CI, 89.2-92.0%) for ruling out APO. Sensitivity was 18.2% (95% CI, 16.3-20.0%). The NPV varied with the population prevalence of APO and was high in very-low-risk settings (NPV, 99.1% (95% CI, 98.9-99.3%) at 1% APO prevalence) and decreased with increasing risk of APO (NPV, 72.1% (95% CI, 67.7-76.1%) at 30% APO prevalence). Temporal proximity of FHR assessment to delivery indicated robust specificity, which was similar for assessments performed at 0-24 h and 24-48 h prior to delivery (specificity at 0-24 h, 90.8% (95% CI, 88.8-92.7%); specificity at 24-48 h, 90.3% (95% CI, 88.2-92.3%); P = 0.898). Across the different adverse outcomes comprising the APO cohort, the performance of the Dawes-Redman algorithm remained consistent, with high specificity (ranging from 87.7% to 94.7%) and NPVs (ranging from 95.4% to 96.0%), confirming its utility in identifying fetal wellbeing.</p><p><strong>Conclusion: </strong>These findings indicate that the Dawes-Redman algorithm is effective for its intended purpose: identifying a state of fetal wellb
目的:通过分析30年的回顾性临床资料,比较正常和不良妊娠结局,评估关键指标,并在分娩前0-48小时测试其性能,评估Dawes-Redman算法在识别足月胎儿健康方面的有效性。方法:从牛津大学医院数据库中提取1991 - 2024年妊娠37 + 0 ~ 41 + 6周足月单胎妊娠的产前胎心率(FHR)。有30%的信号信息缺失或Dawes-Redman分析不完整的痕迹被排除。仅考虑在交货前48小时内进行的跟踪。采用严格的纳入和排除标准,建立了一组妊娠结局正常的妊娠队列。如果新生儿在分娩后经历了7种不良妊娠结局(APO)中的至少一种,则研究另一组有不良妊娠结局(APO)的妊娠。倾向评分匹配(PSM)通过六个因素促进了NPO和APO队列之间的平衡比较:FHR监测时的胎龄、胎儿性别、分娩时的母亲体重指数、分娩时的母亲年龄、胎次和FHR追踪到分娩的时间间隔。根据Dawes-Redman算法,FHR痕迹被分类为“符合标准”(表明胎儿健康)或“不符合标准”(表明需要进一步评估),这为预测性能指标的评估提供了信息。采用准确性、敏感性、特异性、阳性预测值和阴性预测值(NPV)对不同人群的APO风险患病率进行调整,评估疗效。结论:这些发现表明Dawes-Redman算法对于其预期目的是有效的:识别胎儿的健康状态。它的高特异性证明了这一点。然而,它的低灵敏度表明其识别有APO风险的胎儿的能力有限。该算法的预测准确性受到人群中健康怀孕率的显著影响。不符合10个Dawes-Redman标准的FHR痕迹的临床解释需要进一步的专家临床评估。虽然该算法证明其主要目标是可靠的,但针对高危妊娠场景优化算法的开发仍然是未来研究的一个感兴趣的领域。©2025作者。妇产科学超声由John Wiley & Sons Ltd代表国际妇产科学超声学会出版。
{"title":"Performance evaluation of computerized antepartum fetal heart rate monitoring: Dawes-Redman algorithm at term.","authors":"G Davis Jones, B Albert, W Cooke, M Vatish","doi":"10.1002/uog.29167","DOIUrl":"10.1002/uog.29167","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objectives: &lt;/strong&gt;To assess the effectiveness of the Dawes-Redman algorithm in identifying fetal wellbeing at term by analyzing 30 years of retrospective clinical data, comparing normal and adverse pregnancy outcomes, evaluating key metrics and testing its performance when used 0-48 h before delivery.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Antepartum fetal heart rate (FHR) traces from term singleton pregnancies at 37 + 0 to 41 + 6 weeks' gestation obtained between 1991 and 2024 were extracted from the Oxford University Hospitals database. Traces with &gt; 30% of their signal information missing or with incomplete Dawes-Redman analyses were excluded. Only traces performed within 48 h prior to delivery were considered. A cohort of pregnancies with subsequent normal pregnancy outcome (NPO) was established using rigorous inclusion and exclusion criteria. Another cohort of pregnancies with adverse pregnancy outcome (APO) was developed if the neonate experienced at least one of seven APOs after delivery. Propensity score matching (PSM) facilitated a balanced comparison between NPO and APO cohorts using six factors: gestational age at FHR monitoring, fetal sex, maternal body mass index at presentation, maternal age at delivery, parity and time interval between FHR trace and delivery. FHR traces were categorized as either 'criteria met' (indicating fetal wellbeing) or 'criteria not met' (indicating a need for further evaluation) according to the Dawes-Redman algorithm, which informed the evaluation of predictive performance metrics. Performance was assessed using accuracy, sensitivity, specificity, positive predictive value, and negative predictive value (NPV) adjusted for various population risk prevalences of APO.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;A balanced dataset of 3316 antepartum FHR traces was developed with PSM (standardized mean difference &lt; 0.10). The Dawes-Redman algorithm showed a high specificity of 90.7% (95% CI, 89.2-92.0%) for ruling out APO. Sensitivity was 18.2% (95% CI, 16.3-20.0%). The NPV varied with the population prevalence of APO and was high in very-low-risk settings (NPV, 99.1% (95% CI, 98.9-99.3%) at 1% APO prevalence) and decreased with increasing risk of APO (NPV, 72.1% (95% CI, 67.7-76.1%) at 30% APO prevalence). Temporal proximity of FHR assessment to delivery indicated robust specificity, which was similar for assessments performed at 0-24 h and 24-48 h prior to delivery (specificity at 0-24 h, 90.8% (95% CI, 88.8-92.7%); specificity at 24-48 h, 90.3% (95% CI, 88.2-92.3%); P = 0.898). Across the different adverse outcomes comprising the APO cohort, the performance of the Dawes-Redman algorithm remained consistent, with high specificity (ranging from 87.7% to 94.7%) and NPVs (ranging from 95.4% to 96.0%), confirming its utility in identifying fetal wellbeing.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;These findings indicate that the Dawes-Redman algorithm is effective for its intended purpose: identifying a state of fetal wellb","PeriodicalId":23454,"journal":{"name":"Ultrasound in Obstetrics & Gynecology","volume":"65 2","pages":"191-197"},"PeriodicalIF":6.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11788457/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143081178","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Diagnostic accuracy of cell-free fetal DNA in maternal blood in detecting chromosomal anomalies in twin pregnancy: systematic review and meta-analysis. 母血中无细胞 DNA 在检测双胎妊娠染色体异常方面的诊断准确性:系统综述和荟萃分析。
IF 6.3 1区 医学 Q1 ACOUSTICS Pub Date : 2025-02-01 Epub Date: 2025-01-12 DOI: 10.1002/uog.27698
L Della Valle, M Piergianni, A Khalil, A Novelli, G Rizzo, I Mappa, S Prasad, B Matarrelli, V Gatta, L Stuppia, G Pagani, M E Flacco, F D'Antonio

Objective: To report the diagnostic accuracy of cell-free fetal DNA (cfDNA) in maternal blood in detecting fetal chromosomal anomalies in twin pregnancy.

Methods: PubMed, MEDLINE, EMBASE and Cochrane databases were searched from inception to November 2023. The inclusion criteria were twin pregnancy undergoing cfDNA screening for trisomies 21, 18 and 13, monosomy X and/or other sex-chromosome aneuploidies (SCA). The index test was cfDNA screening. The reference standard was pre- or postnatal karyotyping (in the case of a positive cfDNA result) or neonatal phenotypic assessment (in case of a negative cfDNA result). The quality of included studies was assessed using the revised quality assessment of diagnostic accuracy studies (QUADAS-2) tool. Summary estimates of diagnostic accuracy were computed using a bivariate random-effects model.

Results: Thirty-five studies were included in the systematic review and meta-analysis. cfDNA had a high accuracy in detecting trisomy 21 in twin pregnancy, with a sensitivity of 98.8% (95% CI, 96.5-100%) and specificity of 100% (95% CI, 99.9-100%). Sensitivity and specificity were 94.9% (95% CI, 75.9-99.1%) and 100% (95% CI, 99.9-100%), respectively, for trisomy 18 and 84.6% (95% CI, 54.6-98.1%) and 100% (95% CI, 99.9-100%), respectively, for trisomy 13. We could not compute the diagnostic accuracy of cfDNA in detecting monosomy X, owing to an absence of positive cases, while cfDNA had a sensitivity of 100% (95% CI, 71.5-100%) and specificity of 99.8% (95% CI, 99.7-99.9%) for other SCA. The accuracy of cfDNA in detecting the common trisomies was similar in dichorionic and monochorionic twin pregnancies.

Conclusions: cfDNA has high diagnostic accuracy in detecting trisomies 21 and 18 in twin pregnancy, irrespective of chorionicity. Estimation of diagnostic accuracy for trisomy 13 and other SCA was limited by the small number of affected cases and the difficulty associated with detecting false-negative cases of other SCA, and thus requires confirmation in larger studies. © 2024 International Society of Ultrasound in Obstetrics and Gynecology.

目的:报告无细胞 DNA(cfDNA)在检测双胎妊娠染色体异常方面的诊断准确性:报告母血中无细胞 DNA(cfDNA)在检测双胎妊娠染色体异常方面的诊断准确性:方法:检索 Medline、Embase 和 Cochrane 数据库。纳入标准为接受 cfDNA 筛查的双胎妊娠,筛查 13、18、21 三体综合征、X0 单体综合征和其他性染色体异常 (SCA)。指标检测以 cfDNA 检测的阳性结果为代表。参考标准以核型结果(产前或产后获得)为代表,如果 cfDNA 结果为阴性,则以正常新生儿表型为代表。研究质量采用修订后的诊断准确性研究质量评估工具(QUADAS-2)进行评估。使用双变量随机效应模型计算了灵敏度、特异性、阳性和阴性似然比(LR+ 和 LR-)以及诊断几率比(DOR)的简要估计值及相应的 95% 置信区间(95% CI):cfDNA检测双胎妊娠中21三体综合征的准确率很高,灵敏度为98.8%(95% CI 96.5-100),特异性为100%(95% CI 99.9-100)。18 三体综合征的敏感性和特异性分别为 94.9%(95% CI 75.6-99.1)和 100(95% CI 99.9-100),13 三体综合征的敏感性和特异性分别为 84.6%(95% C% 54.6-98.1)和 100%(95% CI 99.9-100)。我们无法计算 cfDNA 检测双胞胎 X0 单体症的诊断准确性,而 cfDNA 检测其他 SCA(11 例)的敏感性为 100%(95% CI 71.5-100),特异性为 99.8%(95% CI 99.7-99.9)。结论:无论绒毛膜性如何,cfDNA 在检测双胎妊娠中的 18 三体综合征和 21 三体综合征方面具有很高的诊断准确性。13三体综合征和SCA的检测准确性因受影响病例的数量较少和SCA假阴性病例的确认困难而受到限制,需要在更大规模的研究中进行确认。本文受版权保护。保留所有权利。
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引用次数: 0
Perinatal diagnosis of renal agenesis in female fetus: implication for investigation of OHVIRA syndrome in adolescence. 女性胎儿肾脏发育不全的围产期诊断:对青少年 OHVIRA 综合征调查的影响。
IF 6.1 1区 医学 Q1 ACOUSTICS Pub Date : 2025-02-01 Epub Date: 2024-07-25 DOI: 10.1002/uog.27714
A Ludwin, L Zaborowska
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引用次数: 0
期刊
Ultrasound in Obstetrics & Gynecology
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